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Infant With Fat-Soluble Vitamin Deficiencies Caused by Cystic FibrosisEmail this article to a colleague. Save this article to My Clippings. Discuss or comment on this article.
A 3-month-old African American boy was referred for evaluation of poor weight gain and vomiting. The infant had been evaluated by his primary care physician 15 times within the past 6 weeks; he had no change in symptoms despite various treatments. (Source: Consultant Live)
Source: Consultant Live - February 9, 2010 Category: Primary Care Source Type: info

(French) Mucoviscidose et fertilitéEmail this article to a colleague. Save this article to My Clippings. Discuss or comment on this article.
Translated by Marie-Claude Falardeau (Source: Cystic Fibrosis Worldwide)
Source: Cystic Fibrosis Worldwide - February 9, 2010 Category: Respiratory Medicine Tags: CFW Newsletter Source Type: organizations

(French) Le groupe international de physiothérapie MucoviscidoseEmail this article to a colleague. Save this article to My Clippings. Discuss or comment on this article.
Translated by Florence Stubbs (Source: Cystic Fibrosis Worldwide)
Source: Cystic Fibrosis Worldwide - February 9, 2010 Category: Respiratory Medicine Tags: CFW Newsletter Source Type: organizations

(French) Breathing for a Living (Respirer pour vivre)Email this article to a colleague. Save this article to My Clippings. Discuss or comment on this article.
Translated by Corinne Boyens (Source: Cystic Fibrosis Worldwide)
Source: Cystic Fibrosis Worldwide - February 9, 2010 Category: Respiratory Medicine Tags: CFW Newsletter Source Type: organizations

(French) Ouverture de la clinique de traitement de la mucoviscidose : Tbilisi, GéorgieEmail this article to a colleague. Save this article to My Clippings. Discuss or comment on this article.
Translated by Corinne Boyens (Source: Cystic Fibrosis Worldwide)
Source: Cystic Fibrosis Worldwide - February 9, 2010 Category: Respiratory Medicine Tags: CFW Newsletter Source Type: organizations

(French) La détection de la délétion complète maintenant possible pour la mucoviscidose avec le AmbrEmail this article to a colleague. Save this article to My Clippings. Discuss or comment on this article.
Translated by Marie-Claude Falardeau (Source: Cystic Fibrosis Worldwide)
Source: Cystic Fibrosis Worldwide - February 9, 2010 Category: Respiratory Medicine Tags: CFW Newsletter Source Type: organizations

The experience of parenting children with chronic health conditions: a new realityEmail this article to a colleague. Save this article to My Clippings. Discuss or comment on this article.
Conclusion. This metasynthesis provides an enhanced empirical understanding of the experiences of people who parent and care for children with chronic health conditions as described by the reviewed literature. While it is apparent that many of these experiences are perceived as negative and undesirable, parents are also noted to describe positive experiences which enhance their lives and give them meaning.Relevance to clinical practice. This metasynthesis provides healthcare professionals with information pertaining to the lived experiences of the parents of children with chronic health conditions. It highlights areas requ...
Source: Journal of Nursing and Healthcare of Chronic Illness - February 9, 2010 Category: Nursing Authors: Elizabeth Kepreotes, Diana Keatinge, Teresa Stone Tags: ARTICLES Source Type: journals

Adapting to clogged airways makes common pathogen resist powerful antibiotics -- even without previous exposureEmail this article to a colleague. Save this article to My Clippings. Discuss or comment on this article.
Certain bacteria cause chronic lung infections in people with cystic fibrosis. Surviving in this oxygen-poor, nitrate-rich environment makes the bacteria less susceptible to antibiotics. (Source: uwnews.org | Health and Medicine)
Source: uwnews.org | Health and Medicine - February 8, 2010 Category: Universities & Medical Training Tags: Health and Medicine Source Type: news

Cystic Fibrosis Foundation Receives $521,000 From BJ's Restaurants, Inc., As Part Of Long-Term Commitment To Fight Life-Threatening DiseaseEmail this article to a colleague. Save this article to My Clippings. Discuss or comment on this article.
As part of a steadfast commitment to finding a cure for cystic fibrosis, BJ's Restaurants, Inc. donated $521,000 to the Cystic Fibrosis Foundation in 2009 for research, care and education programs. BJ's has been involved with the Foundation since 1998 and is one of its largest and most loyal corporate supporters. "We are truly grateful to BJ's restaurants, their team members and their customers for their generosity and desire to help support the Cystic Fibrosis Foundation's mission," said C... (Source: Health News from Medical News Today)
Source: Health News from Medical News Today - February 8, 2010 Category: Consumer Health News Tags: cystic fibrosis Source Type: news

Cystic Fibrosis Foundation Receives $521,000 From BJ's Restaurants, Inc., As Part Of Long-Term Commitment To Fight Life-Threatening DiseaseEmail this article to a colleague. Save this article to My Clippings. Discuss or comment on this article.
As part of a steadfast commitment to finding a cure for cystic fibrosis, BJ's Restaurants, Inc. donated $521,000 to the Cystic Fibrosis Foundation in 2009 for research, care and education programs. BJ's has been involved with the Foundation since 1998 and is one of its largest and most loyal corporate supporters... (Source: Cystic Fibrosis News From Medical News Today)
Source: Cystic Fibrosis News From Medical News Today - February 8, 2010 Category: Respiratory Medicine Tags: cystic fibrosis Source Type: news

Gene test that screens 109 diseases to be offered onlineEmail this article to a colleague. Save this article to My Clippings. Discuss or comment on this article.
The saliva test identifies if a prospective parent is carrying genetic mutations that could cause life-threatening illnesses, like cystic fibrosis or spinal muscular atrophy. (Source: the Mail online | Health)
Source: the Mail online | Health - February 8, 2010 Category: Consumer Health News Source Type: news

What is the Differential Diagnosis of Failure to Thrive?Email this article to a colleague. Save this article to My Clippings. Discuss or comment on this article.
Discussion Failure to Thrive (FTT) is defined as persistent weight below the 3rd percentile for age in infants and young children. The associated terms “Failure to gain weight” (FGW) or “Lack of Normal Physiologic Growth and Development” are more precise, especially for children who are not below the 3rd percentile but are losing weight over time and/or crossing percentile lines on their growth curve. For general growth parameters see How Do I Calculate Mid-Parental Height and Other Growth Parameters? About 70-80% of FTT cases have psychosocial problems that are associated with the FTT or the primar...
Source: PediatricEducation.org - February 8, 2010 Category: Pediatrics Authors: Donna M. D'Alessandro, M.D. Tags: Uncategorized Source Type: info

Low prevalence of glucose intolerance in racially mixed children with cystic fibrosisEmail this article to a colleague. Save this article to My Clippings. Discuss or comment on this article.
Conclusions: The low prevalence of carbohydrate intolerance in this population is probably a result of their young age. Another possibility is the low frequency of the [Delta]F508 mutation. Although not conclusive, these data suggest that in addition to age, the genotype:phenotype ratio may influence the development of glucose intolerance in patients with CF. (Source: Pediatric Diabetes)
Source: Pediatric Diabetes - February 8, 2010 Category: Endocrinology Authors: Crésio Alves, Daniela S Lima, Mauricio Cardeal, Angelica Santana Source Type: journals

Pseudomonas aeruginosa Cystic Fibrosis isolates of similar RAPD genotype exhibit diversity in biofilm forming ability in vitro.Email this article to a colleague. Save this article to My Clippings. Discuss or comment on this article.
Conclusions: Clinical isolates that do not produce biofilms in the laboratory must have the ability to survive in the patient lung. We propose that a synergy exists between isolates in vivo, which allows "non biofilm-forming" isolates to be incorporated into the biofilm. Therefore, there is the potential for strains that are apparently non-biofilm forming in vitro to participate in biofilm-mediated pathogenesis in the CF lung. (Source: BioMed Central)
Source: BioMed Central - February 8, 2010 Category: Journals (General) Authors: Elena DeligianniSally PattisonDaniel BerrarNigel TernanRichard HaylockJohn MooreJ. Stuart ElbornJames Dooley Source Type: journals

CREON(R) (pancrelipase) Delayed-Release Capsules Significantly Improves Fat Absorption In Children With Cystic FibrosisEmail this article to a colleague. Save this article to My Clippings. Discuss or comment on this article.
Solvay Pharmaceuticals, Inc. announced that Phase IIIb data published in the January issue of Clinical Therapeutics confirm that CREON® (pancrelipase) Delayed-Release Capsules significantly improves a key measure of fat absorption in children aged 7-11 years who have exocrine pancreatic insufficiency (EPI) due to cystic fibrosis (CF), EPI is a condition resulting from a deficiency in the production and/or secretion of pancreatic enzymes that are necessary to digest nutrients in food... (Source: Health News from Medical News Today)
Source: Health News from Medical News Today - February 6, 2010 Category: Consumer Health News Tags: cystic fibrosis Source Type: news

Dietary Supplementation with Pressurized Whey in Patients with Cystic FibrosisEmail this article to a colleague. Save this article to My Clippings. Discuss or comment on this article.
Journal of Medicinal Food Feb 2010, Vol. 13, No. 1: 77-82. (Source: Journal of Medicinal Food)
Source: Journal of Medicinal Food - February 6, 2010 Category: Nutrition Tags: article Source Type: journals

CREON (Pancrelipase) Delayed-Release Capsules Significantly Improves Fat Absorption in Children with Cystic Fibrosis, Study in Clinical Therapeutics ReportsEmail this article to a colleague. Save this article to My Clippings. Discuss or comment on this article.
Data CONFIRMS safe and effective use of CREON® in pediATRIC PAtients - MARIETTA, Ga., Feb. 5 /PRNewswire-FirstCall/ -- Solvay Pharmaceuticals, Inc. announced today that Phase IIIb data published in the January issue of Clinical Therapeutics... (Source: Drugs.com - Clinical Trials)
Source: Drugs.com - Clinical Trials - February 5, 2010 Category: Pharmaceuticals Source Type: clinical trials

(French) LA VIE EST UN DEFIEmail this article to a colleague. Save this article to My Clippings. Discuss or comment on this article.
Translated by Patricia PORTETELLE (Source: Cystic Fibrosis Worldwide)
Source: Cystic Fibrosis Worldwide - February 5, 2010 Category: Respiratory Medicine Tags: CFW Newsletter Source Type: organizations

(French) Le dialogue entre le cerveau et le corpsEmail this article to a colleague. Save this article to My Clippings. Discuss or comment on this article.
Translated by Florence Maag (Source: Cystic Fibrosis Worldwide)
Source: Cystic Fibrosis Worldwide - February 5, 2010 Category: Respiratory Medicine Tags: CFW Newsletter Source Type: organizations

(French) La mucoviscidose en BelgiqueEmail this article to a colleague. Save this article to My Clippings. Discuss or comment on this article.
Translated by Marie Claire Britton (Source: Cystic Fibrosis Worldwide)
Source: Cystic Fibrosis Worldwide - February 5, 2010 Category: Respiratory Medicine Tags: CFW Newsletter Source Type: organizations

(French) PERSPECTIVES DE NOUVELLES THERAPIES DE LA MUCOVISCIDOSEEmail this article to a colleague. Save this article to My Clippings. Discuss or comment on this article.
Translated by Benoit TCHUNDJU (Source: Cystic Fibrosis Worldwide)
Source: Cystic Fibrosis Worldwide - February 5, 2010 Category: Respiratory Medicine Tags: CFW Newsletter Source Type: organizations

Transforming Growth Factor {beta}1 Inhibits Cystic Fibrosis Transmembrane Conductance Regulator-dependent cAMP-stimulated Alveolar Epithelial Fluid Transport via a Phosphatidylinositol 3-Kinase-dependent Mechanism [Cell Biology]Email this article to a colleague. Save this article to My Clippings. Discuss or comment on this article.
Exogenous or endogenous β2-adrenergic receptor agonists enhance alveolar epithelial fluid transport via a cAMP-dependent mechanism that protects the lungs from alveolar flooding in acute lung injury. However, impaired alveolar fluid clearance is present in most of the patients with acute lung injury and is associated with increased mortality, although the mechanisms responsible for this inhibition of the alveolar epithelial fluid transport are not completely understood. Here, we found that transforming growth factor β1 (TGF-β1), a critical mediator of acute lung injury, inhibits β2-adrenergic receptor a...
Source: Journal of Biological Chemistry - February 5, 2010 Category: Chemistry Authors: Roux, J., Carles, M., Koh, H., Goolaerts, A., Ganter, M. T., Chesebro, B. B., Howard, M., Houseman, B. T., Finkbeiner, W., Shokat, K. M., Paquet, A. C., Matthay, M. A., Pittet, J.-F. Tags: Cell Biology Source Type: journals

(Dutch) Het leven is juist een uitdagingEmail this article to a colleague. Save this article to My Clippings. Discuss or comment on this article.
Translated by René Knoop (Source: Cystic Fibrosis Worldwide)
Source: Cystic Fibrosis Worldwide - February 5, 2010 Category: Respiratory Medicine Tags: CFW Newsletter Source Type: organizations

(Dutch) CF in BelgiëEmail this article to a colleague. Save this article to My Clippings. Discuss or comment on this article.
Translated by Henny de Lege (Source: Cystic Fibrosis Worldwide)
Source: Cystic Fibrosis Worldwide - February 5, 2010 Category: Respiratory Medicine Tags: CFW Newsletter Source Type: organizations

(Dutch) Breathing for a LivingEmail this article to a colleague. Save this article to My Clippings. Discuss or comment on this article.
Translated by Mariëtte van Drunen (Source: Cystic Fibrosis Worldwide)
Source: Cystic Fibrosis Worldwide - February 5, 2010 Category: Respiratory Medicine Tags: CFW Newsletter Source Type: organizations

(Dutch) De Internationale Fysiotherapie Groep Cystic FibrosisEmail this article to a colleague. Save this article to My Clippings. Discuss or comment on this article.
Translated by Margit Brave (Source: Cystic Fibrosis Worldwide)
Source: Cystic Fibrosis Worldwide - February 5, 2010 Category: Respiratory Medicine Tags: CFW Newsletter Source Type: organizations

Current Clinical Prospects for Gene and Stem Cell Therapies to treat Cystic Fibrosis and other GenetEmail this article to a colleague. Save this article to My Clippings. Discuss or comment on this article.
By Dace Shugg, Bob Williamson (Source: Cystic Fibrosis Worldwide)
Source: Cystic Fibrosis Worldwide - February 5, 2010 Category: Respiratory Medicine Tags: CFW Newsletter Source Type: organizations

The Survival of the (Un)FittestEmail this article to a colleague. Save this article to My Clippings. Discuss or comment on this article.
By Dick Lijnsveld (Source: Cystic Fibrosis Worldwide)
Source: Cystic Fibrosis Worldwide - February 5, 2010 Category: Respiratory Medicine Tags: CFW Newsletter Source Type: organizations

The International Physiotherapy Group Cystic FibrosisEmail this article to a colleague. Save this article to My Clippings. Discuss or comment on this article.
By Brenda Button (Source: Cystic Fibrosis Worldwide)
Source: Cystic Fibrosis Worldwide - February 5, 2010 Category: Respiratory Medicine Tags: CFW Newsletter Source Type: organizations

Cystic fibrosis patients having ChildrenEmail this article to a colleague. Save this article to My Clippings. Discuss or comment on this article.
(Source: Cystic Fibrosis Worldwide)
Source: Cystic Fibrosis Worldwide - February 5, 2010 Category: Respiratory Medicine Tags: CFW Newsletter Source Type: organizations

Air Travel and Lung Disease: Current Guidelines Are InappropriateEmail this article to a colleague. Save this article to My Clippings. Discuss or comment on this article.
(Source: Cystic Fibrosis Worldwide)
Source: Cystic Fibrosis Worldwide - February 5, 2010 Category: Respiratory Medicine Tags: CFW Newsletter Source Type: organizations

Corus Pharma's Phase III Trial for Cystic Fibrosis DrugEmail this article to a colleague. Save this article to My Clippings. Discuss or comment on this article.
(Source: Cystic Fibrosis Worldwide)
Source: Cystic Fibrosis Worldwide - February 5, 2010 Category: Respiratory Medicine Tags: CFW Newsletter Source Type: organizations

Making Music that Makes a DifferenceEmail this article to a colleague. Save this article to My Clippings. Discuss or comment on this article.
(Source: Cystic Fibrosis Worldwide)
Source: Cystic Fibrosis Worldwide - February 5, 2010 Category: Respiratory Medicine Tags: CFW Newsletter Source Type: organizations

Gross Deletion Detection Now Available with the Ambry Test for Cystic FibrosisEmail this article to a colleague. Save this article to My Clippings. Discuss or comment on this article.
(Source: Cystic Fibrosis Worldwide)
Source: Cystic Fibrosis Worldwide - February 5, 2010 Category: Respiratory Medicine Tags: CFW Newsletter Source Type: organizations

Transient elastography in patients with cystic fibrosisEmail this article to a colleague. Save this article to My Clippings. Discuss or comment on this article.
Conclusion Considering the limitations of US and the low risk-benefit rate of liver biopsy in most CF patients, this preliminary study suggests that TE is an attractive non-invasive way to assess and follow-up liver disease in these patients. Content Type Journal ArticleCategory Original ArticleDOI 10.1007/s00247-009-1531-zAuthors Renaud Menten, Cliniques Universitaires St Luc Radiology Avenue Hippocrate 10 Brussels 1200 BelgiumAnissa Leonard, Cliniques Universitaires St Luc Pediatrics Brussels BelgiumPhilippe Clapuyt, Cliniques Universitaires St Luc Radiology Avenue Hippocrate 10 Brussels 1200 Belgium...
Source: Pediatric Radiology - February 5, 2010 Category: Radiology Tags: Pediatric Radiology Source Type: journals

[Editorial] Fabricated or induced illness by carers: a complex conundrumEmail this article to a colleague. Save this article to My Clippings. Discuss or comment on this article.
You are asked to pay a house visit to a young boy whose medical history includes cerebral palsy, cystic fibrosis, diabetes, food allergies, and intolerance to sunlight. However, on examination, you can find nothing wrong with him. On returning to the surgery, you follow-up with the numerous consultants at the various hospitals where the boy attends. They are also baffled. The only common feature is the mother's insistence that the boy is very ill. In this tragic but true case of child maltreatment, which received wide publicity in the UK recently, doctors involved in the boy's management concluded that there was little wro...
Source: LANCET - February 5, 2010 Category: Journals (General) Authors: The Lancet Tags: Editorial Source Type: journals

Transcriptional response of Burkholderia cenocepacia J2315 sessile cells to treatments with high doses of hydrogen peroxide and sodium hypochloriteEmail this article to a colleague. Save this article to My Clippings. Discuss or comment on this article.
Conclusion: These observations have highlighted that sessile B. cenocepacia J2315 cells may alter several pathways in response to exposure to ROS and they have led to the identification of many genes not previously implicated in the stress response of this pathogen. (Source: BMC Genomics - Latest articles)
Source: BMC Genomics - Latest articles - February 5, 2010 Category: Genetics & Stem Cells Authors: Elke PeetersAndrea SassEshwar MahenthiralingamHans NelisTom Coenye Source Type: journals

Feasibility study to inform the design of a randomised controlled trial to eradicate Pseudomonas aeruginosa infection in individuals with Cystic FibrosisEmail this article to a colleague. Save this article to My Clippings. Discuss or comment on this article.
Conclusions: This work demonstrates the importance of feasibility studies in preparation for multicentre clinical trials. It confirmed the uncertainty amongst clinicians and patients about the clinical question, enabled assessment of the number of potentially eligible patients, the proportion of patients and clinicians prepared to participate and aspects of trial design which might encourage this. It showed that a clinical trial was feasible, but only if patients were recruited from across United Kingdom. (Source: Trials)
Source: Trials - February 5, 2010 Category: Journals (General) Authors: Helen HickeyAshley JonesWarren LenneyPaula WilliamsonRosalind Smyth Source Type: journals

"All at Sea": The Experience of Living With Cystic FibrosisEmail this article to a colleague. Save this article to My Clippings. Discuss or comment on this article.
In this qualitative study the researchers explored living with cystic fibrosis (CF)—a chronic, life-threatening, life-limiting disease that demands a relentless regime of daily treatment. The unique challenges and issue for care that CF presents were considered. Utilizing a phenomenological perspective, data drawn from unstructured interviews included narratives and drawings contributed by children, adolescents, young adults, and parents—eight families representing nine young people with CF. In line with van Manen’s approach, four existentials were used to consider a lifeworld in which notions of time, bo...
Source: Qualitative Health Research - February 4, 2010 Category: Global & Universal Authors: Jessup, M., Parkinson, C. Tags: Articles Source Type: journals

MRP transporters as membrane machinery in the bradykinin-inducible export of ATPEmail this article to a colleague. Save this article to My Clippings. Discuss or comment on this article.
Abstract Adenosine triphosphate (ATP) plays the role of an autocrine/paracrine signal molecule in a variety of cells. So far, however, the membrane machinery in the export of intracellular ATP remains poorly understood. Activation of B2-receptor with bradykinin-induced massive release of ATP from cultured taenia coli smooth muscle cells. The evoked release of ATP was unaffected by gap junction hemichannel blockers, such as 18α-glycyrrhetinic acid and Gap 26. Furthermore, the cystic fibrosis transmembrane regulator (CFTR) coupled Cl− channel blockers, CFTR(inh)172, 5-nitro-2-(3-phenylpropylamino)-benzoic a...
Source: Naunyn-Schmiedeberg's Archives of Pharmacology - February 4, 2010 Category: Drugs & Pharmacology Tags: Naunyn-Schmiedeberg's Archives of Pharmacology Source Type: journals

Life is Meant to be a ChallengeEmail this article to a colleague. Save this article to My Clippings. Discuss or comment on this article.
By Peter Oxford (Source: Cystic Fibrosis Worldwide)
Source: Cystic Fibrosis Worldwide - February 4, 2010 Category: Respiratory Medicine Tags: CFW Newsletter Source Type: organizations

The Dialog Between the Brain and the BodyEmail this article to a colleague. Save this article to My Clippings. Discuss or comment on this article.
By Ester Fride (Source: Cystic Fibrosis Worldwide)
Source: Cystic Fibrosis Worldwide - February 4, 2010 Category: Respiratory Medicine Tags: CFW Newsletter Source Type: organizations

CF in BelgiumEmail this article to a colleague. Save this article to My Clippings. Discuss or comment on this article.
By Karleen De Rijcke (Source: Cystic Fibrosis Worldwide)
Source: Cystic Fibrosis Worldwide - February 4, 2010 Category: Respiratory Medicine Tags: CFW Newsletter Source Type: organizations

Towards new Therapies for Cystic FibrosisEmail this article to a colleague. Save this article to My Clippings. Discuss or comment on this article.
By Alan S. Verkman (Source: Cystic Fibrosis Worldwide)
Source: Cystic Fibrosis Worldwide - February 4, 2010 Category: Respiratory Medicine Tags: CFW Newsletter Source Type: organizations

Opening of the CF Clinic: Tbilisi, GeorgiaEmail this article to a colleague. Save this article to My Clippings. Discuss or comment on this article.
(Source: Cystic Fibrosis Worldwide)
Source: Cystic Fibrosis Worldwide - February 4, 2010 Category: Respiratory Medicine Tags: CFW Newsletter Source Type: organizations

Breathing for a LivingEmail this article to a colleague. Save this article to My Clippings. Discuss or comment on this article.
By Dawn Stevens McGuinness (Source: Cystic Fibrosis Worldwide)
Source: Cystic Fibrosis Worldwide - February 4, 2010 Category: Respiratory Medicine Tags: CFW Newsletter Source Type: organizations

Empyema due to a highly transmissible Pseudomonas aeruginosa strain in an adult cystic fibrosis patient.Email this article to a colleague. Save this article to My Clippings. Discuss or comment on this article.
We describe the first case of pleural empyema due to a particularly pathogenic transmissible strain of P. aeruginosa (the Liverpool epidemic strain [LES]) in an adult CF patient. PMID: 20133415 [PubMed - as supplied by publisher] (Source: Journal of Medical Microbiology)
Source: Journal of Medical Microbiology - February 4, 2010 Category: Microbiology Authors: Mohan K, Lakshman V, Fothergill J, Ledson M, Winstanley C, Walshaw M Tags: J Med Microbiol Source Type: journals

Vertex Announces Results from Phase 2a Trial of VX-809 Targeting the Defective Protein Responsible for Cystic FibrosisEmail this article to a colleague. Save this article to My Clippings. Discuss or comment on this article.
-VX-809 was well-tolerated at all dose levels when dosed once daily for 28 days- -Statistically significant changes observed in measurement of sweat chloride suggest increased CFTR activity- -Data support planned combination trial of VX-809 and... (Source: Drugs.com - Clinical Trials)
Source: Drugs.com - Clinical Trials - February 3, 2010 Category: Pharmaceuticals Source Type: clinical trials

(Spanish) EL CORREOEmail this article to a colleague. Save this article to My Clippings. Discuss or comment on this article.
Translated by Martha Rodríguez (Source: Cystic Fibrosis Worldwide)
Source: Cystic Fibrosis Worldwide - February 3, 2010 Category: Respiratory Medicine Tags: CFW Newsletter Source Type: organizations